Synergistic combination of a glyphosate compound and one of DCOIT or OIT or BBIT

ABSTRACT

A synergistic antimicrobial composition containing a glyphosate compound and one of 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one or 2-n-octly-4-isothiazolin-3-one or N-Butyl-1,2-benzisothiazolin-3-one is provided. Also provided is a method of inhibiting the growth of or controlling the growth of microorganisms in a building material by adding such a synergistic antimicrobial composition. Also provided is a coating composition containing such a synergistic antimicrobial composition, and a dry film made from such a coating composition.

This invention relates to combinations of biocides, the combinations having unexpectedly greater activity than would be expected for the use of both of the individual antimicrobial compounds.

Use of combinations of at least two antimicrobial compounds can broaden potential markets, reduce use concentrations and costs, and reduce waste. In some cases, commercial antimicrobial compounds cannot provide effective control of microorganisms, even at high use concentrations, due to weak activity against certain types of microorganisms, e.g., those resistant to some antimicrobial compounds. Combinations of different antimicrobial compounds are sometimes used to provide overall control of microorganisms in a particular end use environment. For example, WO 1998/121962 discloses combinations of 3-iodo-2-propynyl-butylcarbamate and zinc pyrithione, but this reference does not suggest any of the combinations claimed herein. Moreover, there is a need for additional combinations of antimicrobial compounds with relatively low impact on health and/or the environment. The problem addressed by this invention is to provide such additional combinations of antimicrobial compounds.

Antimicrobial compounds are sometimes included in liquid coating compositions that are applied to a substrate and that become dry films. It is desirable that such dry films control surface fungi and algae and that such dry films also present as little adverse effect as possible on health and the environment.

The following is a statement of the invention.

The first aspect of the present invention is a synergistic antimicrobial composition containing a glyphosate compound and one of 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one or 2-n-octly-4-isothiazolin-3-one or N-Butyl-1,2-benzisothiazolin-3-one is provided. A second aspect of the present invention is a method of inhibiting the growth of or controlling the growth of microorganisms in a building material by adding the synergistic antimicrobial composition of the first aspect of the present invention. A third aspect of the present invention is a coating composition containing a synergistic antimicrobial composition of the first aspect of the present invention.

A fourth aspect of the present invention is dry film made from a coating composition of the third aspect of the present invention.

The following is a detailed description of the invention.

As used herein, the following terms have the designated definitions, unless the context clearly indicates otherwise.

The term “antimicrobial compound” refers to a compound capable of inhibiting the growth of or controlling the growth of microorganisms; antimicrobial compounds include bactericides, bacteristats, fungicides, fungistats, algaecides and algistats, depending on the dose level applied, system conditions and the level of microbial control desired. The term “microorganism” includes, for example, fungi (such as yeast and mold), bacteria and algae. The following abbreviations are used throughout the specification: ppm=parts per million by weight (weight/weight), mL=milliliter, ATCC=American Type Culture Collection, and MIC=minimum inhibitory concentration. Unless otherwise specified, temperatures are in degrees centigrade (° C.), and references to percentages are by weight (wt %). Percentages of antimicrobial compounds in the composition of this invention are based on the total weight of active ingredients in the composition, i.e., the antimicrobial compounds themselves, exclusive of any amounts of solvents, carriers, dispersants, stabilizers or other materials which may be present.

As used herein, “DCOIT” is 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one, and “OIT” is 2-n-octly-4-isothiazolin-3-one, and “BBIT” is N-Butyl-1,2-benzisothiazolin-3-one. When a ratio is said herein to be “X:1 or higher,” it is meant that the ratio is Y:1, where Y is X or greater, and when a ratio is said herein to be “X:1 or lower,” it is meant that the ratio is Z:1, where Z is X or less.

Glyphosate is N-(phosphonomethyl)glycine (registry number 1071-83-6). Glyphosate is a known herbicide that is approved in many jurisdictions for use for weed control on food crop plants. One measure of glyphosate's relatively low impact on the environment is shown by its relatively low activity against various algae. Some results showing the activity of glyphosate against various algae are as follows:

Test⁽¹⁾ Algae 72 hr 96 hr 7 day E_(b)C₅₀ green algae 485 mg/l 13.8 mg/l (Selenastrum capricornutum) E_(r)C₅₀ green algae 460 mg/l (Selenastrum capricornutum) EC₅₀ marine algae 1.3 mg/l 0.64 mg/l (Skeletonema costatum) EC₅₀ diatom (Navicula pelliculosa)   42 mg/l EC₅₀ blue-green algae   15 mg/l (Anabaena flos-aquae) ⁽¹⁾Notes: EC_(n)/EC₅₀ Effective Concentration EC_(n) is the concentration of a substance that affects n % of a population in a given period of time. EC₅₀ is widely used since it is the most accurate point in the concentration effect curve. E_(b)C₅₀ Median effective concentration for biomass (algae): The concentration of a substance which reduces by 50% the increase of biomass compared with a control sample, over a specified time period. E_(r)C₅₀ Median effective concentration for growth rate (algae): The concentration of a substance which reduces by 50% the growth rate of algal cells, compared with a control sample, over a specified time period.

The above data show that glyphosate has relatively low impact on algae, which indicates that glyphosate has relatively low impact the environment. This characteristic is considered desirable for an antimicrobial material that may be included in a coating composition.

The present invention involves the use of a glyphosate compound. As used herein “a glyphosate compound” means glyphosate or a glyphosate salt. A glyphosate salt is a metal salt of glyphosate. Suitable metals include alkali metals, alkaline earth metals, and transition metals. Glyphosate salts are preferred over glyphosate. More preferred are transition metal salts of glyphosate; most preferred is zinc glyphosate.

Glyphosate has relatively high solubility in water. This relatively high solubility in water is not preferred for an antimicrobial material that may be included in a coating composition or other building material, because dried coatings and building materials are exposed to water, which could tend to remove a highly soluble compound from the dried coating or the building material. Preferred are glyphosate salts that have solubility in water, at 20° C., of 3 g/l or less; more preferred is 1 g/l or less; more preferred is 0.3 g/l or less.

It is considered that glyphosate salts will have relatively low impact on health and the environment, because it is considered that glyphosate salts will have impact on health and the environment that is similar to the impact of glyphosate.

The present invention involves a composition that contains both a glyphosate compound and one of 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one or 2-n-octly-4-isothiazolin-3-one or N-Butyl-1,2-benzisothiazolin-3-one. It has been surprisingly found that such a composition is synergistically effective as a biocide. It has been especially surprisingly found that compositions that contain both zinc glyphosate and one of DCOIT or OIT BBIT are synergistically effective as biocides. Preferred are compositions that contain both a glyphosate compound and DCOIT. It has been even more especially surprisingly found that compositions that contain both zinc glyphosate and DCOIT are synergistically effective as biocides.

When DCOIT is present, preferably the weight ratio of DCOIT to glyphosate compound is 0.33:1 or higher. When DCOIT is present, preferably the weight ratio of DCOIT to glyphosate compound is 2:1 or lower. When OIT is present, preferably the weight ratio of OIT to glyphosate compound is 0.3:1 to 0.4:1. When BBIT is present, preferably the weight ratio of BBIT to glyphosate compound is from 0.1:1 to 10:1.

If a formulation contains more than one of the listed IT compounds (i.e., DCOIT, OIT, and BBIT), it is useful to consider the sum of the weights of all the listed IT compounds (i.e., the sum of the weight of DCOIT (if it is present) plus the weight of OIT (if it is present) plus the weight of BBIT (if it is present). The preferred ratio of the sum of the weights of all the listed IT compounds to the weight of glyphosate compound is 0.1:1 to 10:1.

The mixture of glyphosate compound and one of DCOIT or OIT or BBIT may be included in a coating composition. Glyphosate compound and one of DCOIT or OIT or BBIT may be added to the coating composition separately or as a mixture or any combination thereof. Preferred coating compositions are liquid. Coating compositions may be aqueous or non-aqueous. Aqueous coating compositions contain 40% or more water by weight, based on the weight of the coating composition.

Among embodiments in which glyphosate compound and one of DCOIT or OIT or BBIT are included in a paint or other coating composition, preferred coating compositions are liquid compositions, especially compositions that contain dispersions of polymers in aqueous media.

In addition to paints and other coating compositions, the biocide combinations of the present invention are particularly useful in preservation of building materials, e.g., adhesives, caulk, joint compound, sealant, wallboard, etc., polymers, plastics, synthetic and natural rubber, paper products, fiberglass sheets, insulation, exterior insulating finishing systems, roofing and flooring felts, building plasters, bricks, mortar, gypsum board, wood products and wood-plastic composites. When a biocide combination of the present invention is present in a building material, it is preferred that some or all of the biocide combination be present at the surface of the building material or near enough to the surface of the building material to inhibit microbial growth on that surface.

In some embodiments, latex paints or other liquid coating compositions are used that contain the biocide combinations disclosed herein.

Coating compositions are designed so that a layer of the coating composition can readily be applied to a substrate and then dried or allowed to dry to form a dry film. Coating compositions contain a binder. Binders contain one or more of the following: one or more polymer, one or more oligomer, and/or one or more monomer. Oligomers and monomers in binders are designed to polymerize and/or crosslink during or after the formation of the dry film. Polymers in a binder may or may not be designed to crosslink during or after the formation of the dry film.

Coating compositions optionally contain one or more pigment. A pigment is a mineral or an organic substance in the form of small solid particles. Pigments provide full or partial opacity to the dry film.

The biocide combinations are useful for preservation of the dry film coating resulting after application of a paint or other liquid coating composition. Preferably, the antimicrobial composition is an aqueous latex paint comprising one or more of the biocide combinations disclosed herein, or the dry film coating resulting from application of the paint to a surface. An aqueous latex paint is an aqueous liquid coating composition in which the binder is an polymer in the form of a latex (i.e., in the form of polymer particles dispersed throughout the water). More preferred are aqueous latex paints in which the binder contains one or more acrylic polymer.

Typically, the amount of the biocide combinations of the present invention to control the growth of microorganisms is from 100 ppm to 10,000 ppm active ingredient. Preferably, the active ingredients of the composition are present in an amount of at least 300 ppm, preferably at least 500 ppm, preferably at least 600 ppm, preferably at least 700 ppm. Preferably, the active ingredients of the composition are present in an amount of no more than 8,000 ppm, preferably no more than 6,000 ppm, preferably no more than 5,000 ppm, preferably no more than 4,000 ppm, preferably no more than 3,000 ppm, preferably no more than 2500 ppm, preferably no more than 2,000 ppm, preferably no more than 1,800 ppm, preferably no more than 1,600 ppm. Concentrations mentioned above are in a liquid composition containing the biocide combinations; biocide levels in the dry film coating will be higher.

The present invention also encompasses a method for preventing microbial growth in building materials, especially in dry film coatings, by incorporating any of the claimed biocide combinations into the materials.

Typically, the antimicrobial compositions are used to inhibit growth of algae and/or fungi.

The composition of the present invention contains a glyphosate compound and one of DCOIT or OIT or BBIT. It is contemplated that some embodiments may contain one or more additional antimicrobial compound.

It is contemplated that zinc glyphosate shows unexpectedly synergistic antimicrobial action in comparison with results that would be expected from a combination of zinc and glyphosic acid.

The following are examples of the present invention.

Zinc Glyphosate was synthesized as follows.

First, pre-preparation was performed as follows. 15-20 g Glyphosate acid was dried in oven at 80-90° C. overnight. A 1 M solution of NaOH in deionized (DI) water was prepared.

Glyphosate solution was made as follows. 200 mL DI water was measured into 600 mL beaker containing stir bar. 15 g Glyphosate acid was slowly added to beaker of water while stirring on stir plate at medium speed. Temperature was raised up to 60-70° C. to dissolve the glyphosate; temperature was monitored with thermometer. 1M NaOH was added to bring pH up to 6.0. The glyphosate dissolved at a pH around 2.4. The mixture was agitated for 5-10 minutes.

A zinc solution was made as follows. 100 mL DI water was measured into 400 mL beaker containing stir bar. 36.25 g Zinc Chloride (Reagent Grade, >98%, Sigma-Aldrich, material #208086) was measured into weigh boat Zinc chloride was slowly added to water in beaker while mixing on stir plate. Solution was heated up to 65° C.

Zinc glyphosate solution was made as follows. Using a 9-inch Pasteur pipette, the zinc solution was added to the glyphosate solution. After each addition of a small amount of zinc solution to glyphosate solution, the precipitate dissolved before further zinc solution was added. When the precipitate would no longer dissolve, pH was adjusted up to 5. Remainder of zinc solution was poured into the glyphosate solution, and the mixture was stirred overnight.

NOTE: controlling the pH of the solution is extremely important for obtaining the desired product. During the preparations reported herein, care was taken not exceed pH value of 5.

Zinc Glyphosate Filtration was performed as follows.

Filtration apparatus was set up using a Buchner funnel and a filter flask connected with a flask seal and hooked up to a water-vacuum pump. A #41 Whatman™ filter paper was placed in the funnel. The pump was turned on, and DI water was poured onto filter paper to create vacuum. The Glyphosate, zinc slurry was slowly poured onto the filter paper and then washed once with hot (approximately 50° C.) DI water, and then rinsed twice with isopropyl alcohol (IPA).

The Zinc Glyphosate Final Preparation was performed as follows.

Filter paper containing zinc glyphosate precipitate was removed and placed in a large Pyrex™ dish. The dish was covered with metal foil, and a few holes were poked in the foil for ventilation. The precipitate was dried in oven at 80-90° C. overnight. The precipitate was then measured out into a pre-massed, clean, labeled glass bottle, and the mass of the precipitate was recorded.

Sample preparation for antimicrobial testing was performed as follows.

A single biocide or blend of biocides was post added into white acrylic latex paint free of biocides to give a maximum total active ingredient/s concentration tested. This paint was then diluted with a biocide free acrylic latex paint to give targeted concentrations for the testing. Depending on the type of biocide blends tested, the total biocides concentrations varies from 400 to 3300 ppm. After biocides addition or dilution, each sample was hand mixed for at least a minute until uniformity was achieved. Each of the paint samples as well as a control sample (containing no biocide) were used to prepare films on black plastic-vinyl chloride/acetate copolymer panels (Leneta Company, Mahwah, N.J.) using a 0.0762 mm (3 mil) bird bar applicator. The panels were thoroughly dried for at least 2 days avoiding direct exposure to sunlight. Square discs (0.5 inch²; 1.27 cm²) were cut out from each panel and were used as the substrate for fungal and algal efficacy tests. This sample size allowed for an agar border when the sample disc was placed into the well of the test plate. Each sample was tested in duplicate.

The test conditions were as follows.

The appropriate media (BOLD'S 3N for Chlorophytes, BG-11 for Cyanobacteria, and PDA for fungi) were used to support microbial growth. The test plates were maintained at room temp (25° C.-26° C.), in a cycled light-dark environment, for four weeks for algae. Plates for fungal challenge tests were maintained at 30° C. for four weeks. At the end of the incubation period the samples were scored for percent area covered by visible microbial growth.

Algal inoculum was as follows.

Medium abbrevi- for Organisms ation Type testing Gloeocapsa sp. Gs ATCC 29159 Unicellular, BG-11 Colonial Cyanobacteria Oscillatoria sp. Os ATCC 29135 Filamentous BG-11 Cyanobacteria Nostoc commune Nc CCAP 1453/29 Unicellular, Bold Cenobial Chlorophyte Trentepohlia Ta + To UTEX LB Filamentous Bold aurea + 429 + Chlorophyte Trentepohlia CCAP 483/4 odorata Chlorella sp. Cs + Ck ATCC 30582 + Unicellular Bold UTEX + ATCC 11468 Chlorophyte Chlorella kessleri Calothrix parientina Cp UTEX LB Filamentous Bold 1952 Cyanobacteria

Fungal inoculum was as follows.

Medium for Organisms abbreviation ATCC# Growth and Testing Aspergillus niger An 9642 PDA Penicillium funiculosum Pf 11797 PDA Cladosporium herbarum Ch 11281 PDA Aureobasidium pullulans Ap 9348 PDA Trichoderma viride Tv 32630 PDA Alternaria alternata Aa 20084 PDA

Algal efficacy was tested as follows (Modified ASTM 5589).

ASTM 5589 is a standard accelerated test method for determining resistance of various coatings (including paints) to algal defacement. To accommodate for high-throughput screening, this method was scaled down from petri plates to 6-well plates. A single coupon was placed with a pair of sterile forceps at the center of the agar plug (on top) with the painted surface facing upwards. Algal inoculums were prepared by mixing equal concentrations (approximately 1×10⁶ cfu/ml) and equal volumes (depending on number of samples to be inoculated) of like growing organisms.

In this synergy study, three pool of mixed algae were prepared as the test inoculum, Gloeocapsa sp. and Oscillatoria sp. a mix of cyanobacteria grown on BG-11 media; Chlorella sp., Chlorella kessleri, and Nostoc commune are unicellular chlorphytes that were mixed and grown on Bold media; Trentepohlia aurea, Tretepohlia odorata, and Calotrix parientina are filamentous algae that were mixed and grown on Bold media.

Each well that contained a tested coupon was inoculated with 400 μl of organism mixture (approximately 1×10⁶ cfu/ml) making sure that the whole surface (paint film as well as the agar surrounding it) was evenly covered. The plates were incubated at room temp (25° C.-26° C.) with cyclic exposure to light (OTT-Lite model #OTL4012P, 40 Watt, 26 KLumen) and dark phases, for a period of four weeks. The total area covered was evaluated at the end of each week according to percent area covered in 5% increments.

Fungal efficacy was tested as follows (Modified ASTM 5590).

ASTM 5590 is a standard accelerated test method for determining resistance of various coatings (including paints) to fungal defacement. To accommodate for high-throughput screening, this method was scaled down from petri plates to 6-well plates. To set up the test, an agar plug was placed at the bottom of each well of the sterile 6-well plate. A single coupon was placed with a pair of sterile forceps at the center of the agar plug (on top) with the painted surface facing upwards. Fungal inoculums were prepared by mixing equal concentrations (approximately 1×10⁶ cfu/ml) and equal volumes (depending on number of samples to be tested) of like growing organisms. For this synergy study, three pools of mixed fungi were prepared as the test inoculum. Cladosporium herbarum was mixed with Trichoderma viride, Aspergillus niger was mixed with Penicillium funiculosum and Alternaria alternata was mixed with Aureobasidium pullulans. Each well was inoculated with 400 microliter of organism mixture (approximately 1×10⁶ cfu/ml) making sure that the whole surface (paint film as well as the agar surrounding it) was evenly covered. The plates were incubated at 30° C. in presence of moisture, for a period of four weeks. The total percent area covered was evaluated and recorded at the end of each week and recorded in increments of 5%.

The Synergy Index calculation was performed as follows.

The SI is calculated based on F. C. Kull et. Al. method (Applied Microbiology, Vol. 9 (1961). In this study, SI was calculated based on the following formula with the minimum inhibitory concentration chosen based on the percent inhibitory exhibited by the individual biocide against each microorganisms tested. SI=Qa/QA+Qb/QB

-   -   Qa=the concentration of Biocide A in the blend     -   QA=The concentration of Biocide A as the only biocide     -   Qb=The concentration of Biocide B in the blend     -   QB=The concentration of Biocide B as the only biocide

SI value of <1 in the formula indicates a synergism of the blended biocides exists.

Note: If any of the active with maximum concentration tested did not exhibit some inhibition, this maximum concentration is used to calculate the estimated SI and a sign of less than (<) is included to take into account that higher concentration of the active is needed to achieve the targeted inhibition

NE=no end point at the concentration tested that will meet the percent inhibition criteria set in each SI calculation.

Compositions listed below that contain both zinc glyphosate and one of DCOIT or OIT or BBIT are examples of the present invention. Other compositions are comparative compositions.

Test results for Zinc Glyphosate and Glyphosic Acid are shown below:

% Inhibition Against Various Organisms Tested Conc. Cs + Cp + Gs + Aa + An + TV + Active ppm Ck + Nc To + Ta Os Ap Pf Ch Zinc 750 100 0 15 40 20 50 Glyphosate 1500 100 0 72.5 47.5 27.5 75 2500 100 0 90 70 30 90 Glyphosic Acid 750 37.5 0 15 7.5 0 2.5 1500 60 10 72.5 20 5 50 2500 80 7.5 90 67.5 10 72.5 Blank 100 100 100 100 100 100

Test Results for Zinc Glyphosate with DCOIT were as follows.

AaTv AnPf ApCh Cp + To + Ta Cs + Ck + Nc Gs + Os 1 Zinc Glyphosate: 1 DCOIT Total conc, ppm 1725 300 575 300 300 300 % inhibition 80 90 40 100 80 100 SI 2.05 0.50 <0.59 0.63 0.63 0.55 1 Zinc Glyphosate: 2 DCOIT Total conc, ppm 222 222 444 222 222 444 % inhibition 60.0 80 70 100 80 70 SI 0.26 0.31 <0.55 0.44 0.44 0.71 1 Zinc Glyphosate: 5 DCOIT Total conc, ppm 690 690 690 690 690 1035 % inhibition 80 80 70 80 100 60 SI 0.81 0.78 <1.03 1.27 1.28 1.42 1 Zinc Glyphosate: 10 DCOIT Total conc, ppm 632.5 632.5 632.5 949 949 949 % inhibition 60 90 90 80 60 70 SI 0.74 0.64 <1.02 1.71 1.71 1.21 3 Zinc Glyphosate: 1 DCOIT Total conc, ppm 412 412 825 412 412 412 % inhibition 70 80 90 80 100 100 SI 0.49 0.84 <0.27 0.93 0.93 0.87 5 Zinc Glyphosate: 1 DCOIT Total conc, ppm 384 825 1650 384 384 384 % inhibition 80 90 70 80 100 100 SI 0.46 1.79 <0.89 0.88 0.88 0.84 10 Zinc Glyphosate: 1 DCOIT Total conc, ppm 825 825 825 825 825 825 % inhibition 80 80 70 100 100 100 SI 1.00 1.88 <0.36 1.95 1.95 1.91 Zinc Glyphosate Total conc, ppm 825 412.5 3300 412.5 412.5 412.5 % inhibition 40 80 0 80 80 80 DCOIT Total conc, ppm 287.5 1150 575 575 575 825.5 % inhibition 40 80 40 80 20 60 Zinc Glyphosate + DCOIT at ratio 1:10 to 10:1 exhibited a synergy. Zinc Glyphosate + DCOIT at ratio 0.33:1 to 2:1 showed broad spectrum synergy.

Test Results for Zinc Glyphosate with OIT were as follows:

AaTv AnPf ApCh Cp + To + Ta Cs + Ck + Nc Gs + Os 1 Zinc Glyph:1 OIT Total conc, ppm 3300 3300 NE 1650 2475 825 % inhibition 40 40 80 85 80 SI <4.17 4.17 2.61 4.38 0.96 1 Zinc Glyph:2 OIT Total conc, ppm 2700 675 1350 1350 2025 1350 % inhibition 60.0 60 40 80 80 80 SI <4.27 1.07 <1.24 1.76 3.14 1.55 1 Zinc Glyphosate:5 OIT Total conc, ppm 2160 2160 NE 540 2160 2160 % inhibition 60 40 80 100 40 SI <4.11 4.11 0.55 2.87 2.44 1 Zinc Glyphosate:10 OIT Total conc, ppm 1980 1485 NE 1980 1980 NE % inhibition 50 40 100 100 SI <4.05 3.04 1.77 2.44 3 Zinc Glyphosate:1 OIT Total conc, ppm 825 825 NE 3300 412 412 % inhibition 55 40 60 85 80 SI <0.65 0.65 6.61 0.86 0.49 5 Zinc Glyphosate:1 OIT Total conc, ppm 3300 1650 NE 3300 1650 825 % inhibition 50 40 70 85 90 SI <2.06 1.03 7.07 3.64 0.99 10 Zinc Glyphosate:1 OIT Total conc, ppm NE 3300 NE 3300 1650 825 % inhibition 50 80 70 80 SI 1.58 7.49 3.80 0.99 Zinc Glyphosate Total conc, ppm 3300 1650 3300 412.5 412.5 825 % inhibition 0 40 0 80 80 80 DCOIT Total conc, ppm 450 450 900 1350 900 900 % inhibition 100 50 40 80 100 80

Test Results for Zinc Glyphosate with BBIT were as follows:

Cp + To + Ta + Cs + Ck + Nc 3 ZnGlyphosate:1BBIT Total conc in pppm 2475 % Inhibition 0 SI <1.0 1 ZnGlyphosate:10BBIT Total conc in pppm 1485 % Inhibition 0 SI <1.04 1 ZnGlyphosate:10BBIT Total conc in pppm 990 % Inhibition 0 SI <0.69 1 ZnGlyphosate:5BBIT Total conc in pppm 1620 % Inhibition 0 SI <0.69 1 ZnGlyphosate:1BBIT Total conc in pppm 1650 % Inhibition 0 SI <0.86 ZnGlyphosate Total conc in pppm 3300 % Inhibition 100, NE BBIT Total conc in pppm 1350 % Inhibition 0 Zinc Glyphosate+BBIT at ratio 1:1 to 3:1 and 1:5 and 1:10 exhibited a synergy. Three more separate studies were conducted with the mixtures of algae: Gs+Os, fast growing fungi: An, Aa, Pf, Tv and slow growing fungi: Ap+Ch. No synergistic effect was observed from those three studies. 

The invention claimed is:
 1. A synergistic antimicrobial composition present in an effective amount to control algae and fungi comprising zinc glyphosate and 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one wherein the weight ratio of the zinc glyphosate to the 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one is from 1:10 to 10:1.
 2. A method of inhibiting growth of or controlling growth of microorganisms in a building material, said method comprising a step of adding the synergistic antimicrobial composition of claim 1 to said building material.
 3. A coating composition comprising the synergistic antimicrobial composition of claim
 1. 4. A dry film made by a process comprising applying a layer of the coating composition of claim 3 to a substrate and allowing said coating composition to dry.
 5. A synergistic antimicrobial composition present in an effective amount to control algae and fungi comprising zinc glyphosate and 2-n-octyl-4-isothiazolin-3-one wherein the weight ratio of the zinc glyphosate to the 2-n-octyl-4-isothiazolin-3-one is 3:1.
 6. A method of inhibiting growth of or controlling growth of microorganisms in a building material, said method comprising a step of adding the synergistic antimicrobial composition of claim 5 to said building material.
 7. A coating composition comprising the synergistic antimicrobial composition of claim
 5. 8. A dry film made by a process comprising applying a layer of the coating composition of claim 7 to a substrate and allowing said coating composition to dry.
 9. A synergistic antimicrobial composition present in an effective amount to control algae and fungi comprising zinc glyphosate and N-Butyl-1,2-benzisothiazolin-3-one wherein the weight ratio of the zinc glyphosate to the N-Butyl-1,2-benzisothiazolin-3-one is from 1:1 to 1:10.
 10. A method of inhibiting growth of or controlling growth of microorganisms in a building material, said method comprising a step of adding the synergistic antimicrobial composition of claim 9 to said building material.
 11. A coating composition comprising the synergistic antimicrobial composition of claim
 9. 12. A dry film made by a process comprising applying a layer of the coating composition of claim 11 to a substrate and allowing said coating composition to dry. 